Allele Registry

Canonical Allele Identifier: PA2827263431

Gene: FCGR3A HGNC NCBI

ClinVar Allele:

227742

ClinVar RCV:

RCV000455498

ClinVar Variation:

225994

HGVS (amino-acid)	Matching Registered Transcripts
NP_001316049.1:p.Phe176Val	CA1211378 NM_001329120.2:c.526T>G